Covid 19 Research using Clinical Trials (Home Page)
BI 706321Wiki
Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation
Correlated Drug Terms (3)
Correlated MeSH Terms (7)
There is one clinical trial.
Clinical Trials
The main objectives are:
- Part I: To investigate safety, tolerability, and pharmacokinetics (PK) of BI 706321 in
healthy male subjects following oral administration of single rising doses.
- Part II: The relative bioavailability of BI 706321 after administration of tablets and
capsules under fasted conditions will be compared with each other and the effect of food
on the tablet bioavailability will be investigated.
NCT03971695 Healthy Drug: BI 706321 Drug: Placebo
Primary Outcomes
Measure: Part I: Safety and tolerability of BI 706321 is the percentage of subjects with drug-related adverse events Time: Up to 22 Days
Measure: Part II: AUC0-tz (area under the concentration-time curve of BI 706321 in plasma over the time interval from 0 to the last quantifiable data point) Time: Up to 22 Days
Measure: Part II: Cmax (maximum measured concentration of BI 706321 in plasma) Time: Up to 22 Days
Secondary Outcomes
Measure: Part I: AUC0-∞ (area under the concentration-time curve of BI 706321 in plasma over the time interval from 0 extrapolated to infinity) Time: Up to 22 Days
Measure: Part I: Cmax (maximum measured concentration of BI 706321 in plasma) Time: Up to 22 Days
Measure: Part I: tmax (time from dosing to the maximum measured concentration of BI 706321 in plasma) Time: Up to 22 Days
Measure: Part II: AUC0-∞ (area under the concentration-time curve of BI 706321 in plasma over the time interval from 0 extrapolated to infinity) Time: Up to 22 Days
No related HPO nodes (Using clinical trials)